EP0164961A2 - Photographic elements employing novel coupler solvents - Google Patents

Abstract

Photograpic coupler solvents having at least one terminal epoxy group and at least one ester or amide group are described for incorporation in photographic emulsions and elements. The solvents are preferably employed in the magenta layer to reduce background stain production by explosure to light, heat and humidity.

Description

• This invention relates to silver halide photographic elements employing novel coupler solvents.
• Images are commonly obtained in the photographic art by a coupling reaction between the development product of a silver halide color developing agent (i.e., oxidized aromatic primary amino developing agent) and a color forming compound commonly referred to as a coupler. The dyes produced by coupling are indoaniline, azomethine, indamine or indophenol dyes, depending upon the chemical composition of the coupler and the developing agent. The subtractive process of color formation is ordinarily employed in multicolor photographic elements and the resulting image dyes are usually cyan, magenta and yellow dyes which are formed in or adjacent silver halide layers sensitive to radiation complementary to the radiation absorbed by the image dye; i.e. silver halide emulsions sensitive to red, green and blue radiation.
• When intended for incorporation in photographic elements, couplers are commonly dispersed therein with the aid of a high boiling organic solvent, referred to as a coupler solvent. Couplers are rendered nondiffusible in photographic elements, and compatible with coupler solvents, by including in the coupler molecule a group referred to as a ballast group. This group is located on the coupler in a position other than the coupling position and imparts to the coupler sufficient bulk to render the coupler nondiffusible in the element as coated and during processing. It will be appreciated that the size and nature of the ballast group will depend upon the bulk of the unballasted coupler and the presence of other substituents on the coupler.
• The high boiling solvents of phthalic ester compounds. e.g. dibutyl phthalate. and phosphoric ester compounds, e.g.. tricresyl phosphate, have often been used as coupler solvents because of their coupler-dispersing ability, inexpensiveness and availability. Such compounds are described in Jelley et al. U.S. Patent 2,322.027. However, a problem exists with using these conventional coupler solvents in that the dye images which are produced may exhibit a tendency to form background stain upon exposure to light, heat and humidity. The problem is even more severe for some of the newer magenta couplers which have increased activity.
• U.S. Patent 4.239,851 relates to cyan couplers which are dissolved in certain epoxy compounds having a particular formula. A problem exists in using these coupler solvents of yellow stain formation on high humidity keeping, stain on exposure to heat or light, and heat fading of the image dye. As will be shown by comparative data hereafter, the compounds of the invention have substantially improved properties in this regard as compared to the closest related epoxy compound of this patent.
• According to the present invention there is provided a photographic element comprising a support having thereon at least one silver halide emulsion layer having associated therewith a-dye-forming coupler dispersed in a coupler solvent therefor characterized in that said coupler solvent has at least one terminal epoxy group and at least one ester or amide group.
• The present invention can provide a photographic element in which undesirable staining effects formed on exposure to heat, light and high humidity, are markedly reduced as compared to coupler solvents of the prior art. and improved stability of the dye image is also obtained.
• The expression "terminal epoxy group" means that the compound has an appendage, either in the middle or at the end, which contains a group having the formula

  

  wherein R is defined hereinafter.
• In a preferred embodiment of the invention the coupler solvents have the formula I.

  

  wherein
• A is a polyvalent atom for example oxygen. nitrogen, sulfur, boron, carbon, phosphorus or silicon;
• an acidic oxide group for example
  
• a carbocyclic group for example benzene. naphthalene, cyclohexane, cyclopentane, cycloheptane or cyclooctane:
• a heterocyclic moiety for example pyridine. pyridine oxide, furan, thiophene, pyrazole. triazine. quinoline. pyran,
  
  or
• an alkane or substituted alkane group such as (̵CH₂)̵_m where m is 1 to 6.
  
  each L is at least one divalent linking group for example
  
  
  or carboxylic esters for example
  
• each R is H. alkyl of 1 to 10 carbon atoms, cycloalkyl for example cyclohexyl. cyclopentyl or cycloheptyl; aryl for example phenyl, tolyl. or naphthyl: heterocycyl for example pyridyl, thienyl, or furyl: COOR₁ wherein R₁ is alkyl of 1 to 20 carbon atoms, or can be taken together with A or L to form a ring for example
  
  R₂ may be hydrogen, alkyl of 1 to 10 carbon atoms. aryl for example phenyl. tolyl or naphthyl: or heterocyclyl for example pyridyl. thienyl or furyl: and
• n is a positive integer of at least one, preferably from 2-4,
• with the proviso that at least one A, L or R contains at least one ester or amide group derived from an acidic oxide of carbon, phosphorous, sulfur, boron or silicon, such as
  
  
  and the like, where Y may be 0 or NR². Each of A, L or R may also be further substituted if desired.
• In a preferred embodiment of the invention, the dye-forming coupler associated with the silver halide emulsion described above forms a magenta dye upon reaction with oxidized color developing agent, and the coupler and coupler solvent are located in the silver halide emulsion layer.
• In another preferred embodiment of the invention, the coupler solvent has the formula II.

  

  wherein
• A¹ is an alkane or substituted alkane group or a carbocyclic group,
• L¹ is a carboxylic ester, and
• n is a positive integer of at least one.
• Preferred compounds included within the scope of the invention include the following:

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  

  
• The above compounds `may be synthesized by forming the ester (or amide) from the corresponding acid chloride and an alcohol (or amine) so that the product contains one or more terminal vinyl groups. Each terminal vinyl group is then oxidized to the corresponding epoxide.
• The coupler solvents of this invention can be used in the ways and for the purposes that coupler solvents are used in the photographic art.
• Typically, the coupler solvent and coupler are incorporated in a silver halide emulsion and the emulsion coated on a support to form a photographic element. Alternatively, the coupler solvent and coupler can be incorporated in photographic elements adjacent the silver halide emulsion where, during development, the coupler will be in reactive association with development products such as oxidized color developing agent. Thus, as used herein, the term "associated therewith" signifies that the coupler solvent and coupler are in the silver halide emulsion layer or in an adjacent location where, during processing, they will come into reactive association with silver halide development products.
• Photographic elements of the invention can be single color elements or multicolor elements. Multicolor elements contain dye image-forming units sensitive to each of the three primary regions of the visible spectrum. Each unit can be comprised of a single emulsion layer or of multiple emulsion layers sensitive to a given region of the spectrum. The layers of the element, including the layers of the image-forming units, can be arranged in various orders as known in the art. In an alternative format, the emulsions sensitive to each of the three primary regions of the spectrum can be disposed as a single segmented layer, e.g., as by the use of microvessels as described in Whitmore U.S. Patent 4,362,806 issued December 7, 1982.
• A typical multicolor photographic element of the invention would comprise a support having thereon a cyan dye image-forming unit comprised of at least one red-sensitive silver halide emulsion layer having associated therewith at least one cyan dye-forming coupler, a magenta dye image-forming unit comprising at least one green-sensitive silver halide emulsion layer having associated therewith at least one magenta dye-forming coupler and a yellow dye image-forming unit comprising at least one blue-sensitive silver halide emulsion layer having associated therewith at least one yellow dye-forming coupler, at least one of the couplers in the element being dissolved in a coupler solvent of this invention. The element can contain additional layers, such as filter layers, interlayers, overcoat layers, subbing layers, and the like.
• The silver halide emulsions employed in the elements of this invention can be either negative-working or positive-working. With negative working silver halide, the processing step gives a negative image. To obtain a positive (or reversal) image, this step can be preceded by development with a non-chromogenic developing agent to develop exposed silver halide, but not form dye, and then uniformly fogging the element to render unexposed silver halide developable. Alternatively, a direct positive emulsion can be employed to obtain a positive image.
• Development is followed by the conventional steps of bleaching, fixing, or bleach-fixing, to remove silver and silver halide, washing and drying.
• The following examples are included for a further understanding of this invention.
Example 1 - Preparation of Compound 2
• A 50.76 g (0.25 mol) portion of phthaloyl chloride (A) was added dropwise under nitrogen to ice cold 93.67 g (0.55 mol) 10-undecen-l-ol (B). Stirring was continued one hour and the mixture was then heated to reflux 45 minutes. Chromatography and distillation gave 58 g pure ester C, b.p. 210°C (0.5 mm).

  

  
Compound 2
• To a stirred, ice cold solution of 16 g (0.034 mol) C in 70 ml dichloromethane was added dropwise a solution of 14.24 g (0.072 mol) m-chloroperbenzoic acid in 130 ml dichloromethane. After one hour, the mixture was washed with a 10% sodium sulfite solution, then with saturated salt solution, dried, and purified by chromatography to give 10.7 g of compound 2.
Example 2 - Preparation of Compound 9, 2-Ethylhexyl 10,11-Epoxyundecanoate
• To a stirred solution of 32.56 g (0.25 mol) 2-ethylhexanol in 100 ml tetrahydrofuran under nitrogen was added slowly over 5 minutes 50.70 g (0.25 mol) 10-undecenoyl chloride (E). After 4 days the mixture was drowned with water, extracted with ethyl acetate, and the extracts washed and dried over magnesium sulfate. Solvent removal gave 70.3 g orange oil with an nmr spectrum consistent with ester F.
• - -To an ice-cold stirred solution of 35 g (0.12 mol) ester F in 200 ml dichloromethane was added dropwise over 15 minutes and under nitrogen a solution of 40.73 g (0.24 mol) m-chloroperbenzoic acid in 450 ml dichloromethane. After 17 hours, 40 . ml water was added dropwise under nitrogen. The mixture was then poured into 300 ml water and the separated organic layer washed with saturated sodium chloride and 10% sodium sulfite solutions then dried over magnesium sulfate. The solvent was removed and the product, redissolved in ethyl acetate, was treated one hour with 20% sodium bicarbonate solution, then washed and dried over magnesium sulfate. Purification by silica gel chromatography and solvent removal yielded a clear oil with an nmr spectrum consistent with expected compound 9.

  
Example 3 - Preparation of Compound 10, 1,2-Bis(10,11-epoxyundecanoyloxy) ethane
• In a procedure similar to that described in Example 2, 6.21 g (0.1 mol) ethylene glycol was converted to the diester G yielding 28 g orange oil after silica gel chromatography. Epoxidation and purification by silica gel chromatography yielded compound 10 as a light yellow waxy solid, m.p. 39-40°C, having the expected nmr spectrum.

  
• Compounds 38 and 39 can be prepared in the same manner as compound 10, wherein A =

  

  respectively.
Example 4 - Preparation of Compound 38, 1,4-Bis-(10,11-epoxyundecanoyloxymethyl)-cyclohexane
• Using the procedure described in Example 3, 21.63 g (0.15 mol) 1,4-cyclohexanedimethanol was esterified to yield 80.9 g orange oil G
• 
• Epoxidation of 40 g G diester and purification yielded a light yellow oil having the nmr spectrum expected for compound 38.
Example 5 - Preparation of Compound 39; p-Phenylene Bis(10,11-epoxyundecanoate)
• The procedure described in Example 3 was employed to convert 16.52 g (0.15 mol) hydroquinone to 34 g diester G

  

  as a white solid, with the correct nmr spectrum after recrystallization from acetonitrile. Epoxidation of 18 g G yielded a white solid with a clearly defined nmr spectrum consistent with compound 39.
Example 6 - Magenta Monolayer Comparative Photographic Test
• A photographic element was prepared by coating a paper support with a photosensitive layer containing a silver bromoiodide emulsion at 3.89 mmols Ag/m², gelatin at 1.615 g/m², and the magenta coupler, coupler solvent and chromanol stabilizer levels indicated in Table 1. The photosensitive layer was overcoated with a layer containing gelatin at 1.08 g/m² and bis-vinylsulfonylmethyl ether at 1.75 weight percent based on total gelatin.
• Samples of each element were imagewise exposed through a graduated-density test object, processed at 33°C employing the color developer identified below, then 1.5 minutes in the bleach-fix bath, washed and dried.

  

  
• The samples were then subjected to three different tests. The "dark fade" test conditions consisted of a "wet oven" (6 weeks at 60°C and 70% R.H.) and a "dry oven" (2 weeks at 77°C, 15% R.H.). The "light fade" test conditions consisted of 24 weeks exposure to 5.4 Klux visible light. A Wratten 2B filter was used to screen the ultraviolet component of incident light from the xenon source. Measurements were made of increases in yellow stain (ΔD_min to blue light) and of changes in a magenta D⁼1.0 patch (ΔD _max to green light). The following results were obtained:

  

  
• It can be seen from magenta layer data in Table 1 that the coupler solvents of the invention are markedly better than either conventional solvents or comparative epoxy coupler solvents in preventing yellow stain formation on high humidity keeping (wet oven). Advantages in limiting stain on exposure to heat (dry oven) or light (light fade) are also noted, especially for compound 2, while control 4 usually increases stain. Resistance to heat fading (dry oven) of the magenta image is also improved by the use of the inventive solvents when the usual stabilizers are present, while fading by humidity (wet oven) and light (light fade) are less affected. Even in the absence of stabilizer, compound 2 shows an improvement in light fading for the dye from coupler 3.
Couplers
• 

  

  

  
Comparative Coupler Solvents
• 

  

  

  
Chromanol Stabilizers
• 

  
Example 7 - Yellow and Cyan Monolayer Photographic Testing
• Coating, processing and testing were carried out as in Example 6 except that yellow and cyan couplers were dispersed without stabilizers and lower levels of silver were employed as noted in Tables 2 and 3. Measurements were made of increases in yellow stain (ΔD_min to blue light) and of changes in a D=1.0 patch for yellow (ΔD_max to blue light) in Table 2 and for cyan (ΔD _max to red light) in Table 3. The following results were obtained:
• 

  
• The data in Tables 2 and 3 show that the inventive coupler solvent compound 2 can replace dibutyl phthalate without detriment in a yellow layer and can give a marked improvement in cyan dye stability to heat and, for a coupler 6 coating, to humidity. Minor improvements in yellow stain limitation for the cyan layers can also be seen under high humidity, heat, and light exposure conditions.

  

  

  

  Example 8 - Magenta Image Granularity Dependence on
Coupler Solvent
• Stepped magenta image samples obtained in Example 6 for coatings of coupler 1 dispersed in three different coupler solvents were examined. Comments on results of the visual examination and granularity measurements are reported in Table 4. The general theory and procedure for measuring Wiener power spectra are described in Chapter 8 of Image Science by J. C. Dainty and R. Shaw, N.Y., Academic Press, 1974. Samples were illuminated diffusely with a Quartz-Halogen lamp (color temperature 3250⁰K) and read through a 25 x 2500pm slit using a Wratten 61 filter and an S-4 phosphor photomultiplier tube. The measurements were adjusted for the frequency sensitivity of the human eye and compared at a density to green light of 0.115.

  
• It is apparent from these data that the undesirable roughness and haziness of images formed using the comparison epoxy coupler solvent compound 4 is evidenced by its much higher granularity than the conventional dibutyl phthalate sample or the even lower granularity sample obtained with coupler solvent compound 2 of this invention. Comparison solvent control 4 gave very viscous dispersions which tended to crystallize and led to non-uniform coatings. Coupler solvents of the invention were free of such problems.
Example 9 - Photographic Test
• A photographic element was prepared by coating a paper support with a photosensitive layer containing a silver bromoiodide emulsion at 3.89 mmoles Ag/m², gelatin at 1.615 g/m², the magenta coupler, coupler solvent and chromanol stabilizer identified in-Table 5 and 10% by coupler weight of diisooctylhydroquinone. The photosensitive layer was overcoated with 861 mg/m2 of a mixed Tinuvin* UV absorber and a gelatin overcoat as in Example 6.
• Samples of each element were exposed and processed as in Example 6. The samples were then subjected to the same accelerated keeping tests as in Example 6. The following results were obtained:

  

  
• The results in Table 5 show that in all cases, inventive coupler solvent compound 2 is more effective than conventional coupler solvents in limiting background stain formation on extended exposure to humidity, heat, or light. In most cases, coupler solvent compound 2 also slightly decreased the Green ΔD_max. With conventional coupler solvents, the choice of stabilizer can give wide variations in stain formation, while with coupler solvent compound 2, various stabilizers can be used advantageously with minimal stain.
Chromanol Stabilizer
• 

  

  

Claims (12)

1. A photographic element comprising a support having thereon at least one silver halide emulsion layer having associated therewith a dye-forming coupler dispersed in a coupler solvent therefor characterized in that said coupler solvent has at least one terminal epoxy group and at least one ester or amide group.

2. The element of claim 1 wherein said coupler solvent has the formula:

wherein

A is a polyvalent atom, an acidic oxide group, a carbocyclic group, a heterocyclic moiety, or an alkane or substituted alkane group;

each L is at least one divalent linking group;

each R is H, alkyl, cycloalkyl, aryl, heterocyclyl, COOR¹, wherein R¹ is alkyl of 1 to 20 carbon atoms, or can be taken together with A or L to form a ring; and

n is a positive integer of at least one, with the proviso that at least one A, L or R contains at least one ester or amide group derived from an acidic oxide of carbon, phosphorous, sulfur, boron or silicon.

3. The element of claim 2 wherein said dye-forming coupler forms a magenta dye upon reaction with oxidized color developing agent.

4. The element of claim 3 wherein said magenta dye-forming coupler is a pyrazolone, pyrazolotriazole, pyrazolobenzimidazole or indazolone, and said coupler and said coupler solvent are located in said silver halide emulsion layer.

5. The element of claim 2 wherein said coupler solvent has the formula:

wherein A¹ is an alkane or substituted alkane group or a carbocyclic group, L¹ is a carboxylic ester and n is a positive integer of at least one.

6. The element of claim 2 wherein said polyvalent atom is oxygen, nitrogen, sulfur, boron, carbon, phosphorus or silicon; said acidic oxide group is

said carbocyclic group is benzene, naphthalene, cyclohexane, cyclopentane, cycloheptane or cyclooctane; said heterocyclic moiety is pyridine, pyridine oxide, furan, thiophene, pyrazole, triazine, quinoline, pyran,

and said alkane or substituted alkane group is (̵CH₂)̵_m where m is 1 to 6,

7. The element of claim 2 wherein said L is (̵CH₂)̵p where p is 1 to 9, -0-, -NH-,

8. The element of claim 2 wherein said ester or amide group is

where Y is 0 or NR² and R² is hydrogen, alkyl, aryl or heterocyclyl.

9. The element of claim 5 wherein A¹ is a benzene ring, n is 2 and each L¹ is

10. The element of claim 5 wherein A¹ is a cyclohexane ring, n is 2 and each L¹ is

11. The element of claim 5 wherein A¹ is

and n is 1.

12. The element of claim 5 wherein A¹ is -CH₂CH₂-, n is 2 and each L¹ is